首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Trace humic and fulvic acid determination in natural water by cloud point extraction/preconcentration using non-ionic and cationic surfactants with FI-UV detection
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Trace humic and fulvic acid determination in natural water by cloud point extraction/preconcentration using non-ionic and cationic surfactants with FI-UV detection

机译:使用非离子和阳离子表面活性剂,通过FI-UV检测,通过浊点萃取/预浓缩,可测定天然水中的痕量腐殖酸和黄腐酸

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A preconcentration and determination method for humic and fulvic acids at trace levels in natural water samples was developed. Cloud point extraction was successfully employed for the preconcentration of humic acid ( HA) and fulvic acid ( FA) prior to the determination by using a flow injection (FI) system coupled to a spectrophotometric UV-Vis detector. The quantitative extraction of HA and FA within the pH range 1 - 12 was obtained by neutralization of the anionic charge on the humic substances with a cationic surfactant, hexadecyltrimethylammonium bromide ( CTAB). This generated a hydrophobic species that was subsequently incorporated ( solubilized) into the micelles of a non-ionic surfactant polyethylene glycol, tert-octylphenyl ether ( Triton X-114). The FI method for HA and FA determination was developed by injection of 100 mul of the extracted surfactant-rich phase using an HPLC pump with spectrophotometric detection at 350 nm. A 50 ml sample solution preconcentration allowed an enrichment factor of 167. The limit of detection (LOD) obtained under the optimal conditions was 5 mug l(-1). The precision for ten replicate determinations at 0.2 mg l(-1) HA was 3.1% relative standard deviation (RSD), calculated from the peak heights. The calibration using the preconcentration system for HA and FA was linear with a correlation coefficient (r(2)) of 0.9997 at levels near the detection limits up to at least 1 mg l(-1). The method was successfully applied to the determination of HA and FA in natural water samples (river water). [References: 41]
机译:建立了天然水样中痕量腐殖酸和黄腐酸的富集和测定方法。在测定之前,通过使用与分光光度法UV-Vis检测器耦合的流动注射(FI)系统,浊点萃取已成功用于腐殖酸(HA)和黄腐酸(FA)的预浓缩。通过用阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)中和腐殖质上的阴离子电荷,可以定量提取pH值为1-12的HA和FA。这产生了疏水物质,该疏水物质随后被结合(增溶)到非离子表面活性剂聚乙二醇叔辛基苯基醚(Triton X-114)的胶束中。通过使用HPLC泵在350 nm处进行分光光度检测,注入100 mul提取的富表面活性剂富集相,开发出用于HA和FA测定的FI方法。 50 ml样品溶液的预浓缩允许富集因子为167。在最佳条件下获得的检测极限(LOD)为5杯l(-1)。根据峰高计算,在0.2 mg l(-1)HA下进行十次重复测定的精密度为3.1%相对标准偏差(RSD)。使用预浓缩系统对HA和FA进行的校准是线性的,相关系数(r(2))为0.9997,在接近检出限(至少1 mg l(-1))的水平上。该方法已成功应用于天然水样品(河流水)中HA和FA的测定。 [参考:41]

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